Previous Article | Next Article 
J Virol, May 1998, p. 4281-4287, Vol. 72, No. 5
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
fus-1, a pH Shift Mutant of Semliki Forest Virus, Acts
by Altering Spike Subunit Interactions via a Mutation in the E2
Subunit
Sallie
Glomb-Reinmund and
Margaret
Kielian*
Department of Cell Biology, Albert Einstein
College of Medicine, Bronx, New York 10461
Received 22 October 1997/Accepted 23 January 1998
Semliki Forest virus (SFV), an enveloped alphavirus, is a
well-characterized paradigm for viruses that infect cells via endocytic uptake and low-pH-triggered fusion. The SFV spike protein is composed of a dimer of E1 and E2 transmembrane subunits, which dissociate upon
exposure to low pH, liberating E2 and the fusogenic E1 subunit to
undergo independent conformational changes. SFV fusion and infection
are blocked by agents such as ammonium chloride, which act by raising
the pH in the endosome and inhibiting the low-pH-induced conformational
changes in the SFV spike protein. We have previously isolated an SFV
mutant, fus-1, that requires more acidic pH to trigger its
fusion activity and is therefore more sensitive to inhibition by
ammonium chloride. The acid shift in the fusion activity of
fus-1 was here shown to be due to a more acidic pH threshold for the initial dissociation of the fus-1 spike
dimer, thereby resulting in a more acidic pH requirement for the
subsequent conformational changes in both fus-1 E1 and
fus-1 E2. Sequence analysis demonstrated that the
fus-1 phenotype was due to a mutation in the E2 spike
subunit, threonine 12 to isoleucine. fus-1 revertants that
have regained the parental fusion phenotype and ammonium chloride
sensitivity were shown to have also regained E2 threonine 12. Our
results identify a region of the SFV E2 spike protein subunit that
regulates the pH dependence of E1-catalyzed fusion by controlling the
dissociation of the E1/E2 dimer.
*
Corresponding author. Mailing address: Department of
Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park
Ave., Bronx, NY 10461. Phone: (718) 430-3638. Fax: (718) 430-8574. E-mail: kielian{at}aecom.yu.edu.
J Virol, May 1998, p. 4281-4287, Vol. 72, No. 5
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Qin, Z.-l., Zheng, Y., Kielian, M.
(2009). Role of Conserved Histidine Residues in the Low-pH Dependence of the Semliki Forest Virus Fusion Protein. J. Virol.
83: 4670-4677
[Abstract]
[Full Text]
-
Wu, S.-R., Haag, L., Sjoberg, M., Garoff, H., Hammar, L.
(2008). The Dynamic Envelope of a Fusion Class II Virus: E3 DOMAIN OF GLYCOPROTEIN E2 PRECURSOR IN SEMLIKI FOREST VIRUS PROVIDES A UNIQUE CONTACT WITH THE FUSION PROTEIN E1. J. Biol. Chem.
283: 26452-26460
[Abstract]
[Full Text]
-
Taylor, G. M., Hanson, P. I., Kielian, M.
(2007). Ubiquitin Depletion and Dominant-Negative VPS4 Inhibit Rhabdovirus Budding without Affecting Alphavirus Budding. J. Virol.
81: 13631-13639
[Abstract]
[Full Text]
-
Liao, M., Kielian, M.
(2006). Functions of the Stem Region of the Semliki Forest Virus Fusion Protein during Virus Fusion and Assembly. J. Virol.
80: 11362-11369
[Abstract]
[Full Text]
-
Liao, M., Kielian, M.
(2006). Site-Directed Antibodies against the Stem Region Reveal Low pH-Induced Conformational Changes of the Semliki Forest Virus Fusion Protein. J. Virol.
80: 9599-9607
[Abstract]
[Full Text]
-
Zhang, X., Fugere, M., Day, R., Kielian, M.
(2003). Furin Processing and Proteolytic Activation of Semliki Forest Virus. J. Virol.
77: 2981-2989
[Abstract]
[Full Text]
-
Hammar, L., Markarian, S., Haag, L., Lankinen, H., Salmi, A., Cheng, R. H.
(2003). Prefusion Rearrangements Resulting in Fusion Peptide Exposure in Semliki Forest Virus. J. Biol. Chem.
278: 7189-7198
[Abstract]
[Full Text]
-
Lee, P., Knight, R., Smit, J. M., Wilschut, J., Griffin, D. E.
(2002). A Single Mutation in the E2 Glycoprotein Important for Neurovirulence Influences Binding of Sindbis Virus to Neuroblastoma Cells. J. Virol.
76: 6302-6310
[Abstract]
[Full Text]
-
Gibbons, D. L., Kielian, M.
(2002). Molecular Dissection of the Semliki Forest Virus Homotrimer Reveals Two Functionally Distinct Regions of the Fusion Protein. J. Virol.
76: 1194-1205
[Abstract]
[Full Text]
-
Lu, Y. E., Eng, C. H., Shome, S. G., Kielian, M.
(2001). In Vivo Generation and Characterization of a Soluble Form of the Semliki Forest Virus Fusion Protein. J. Virol.
75: 8329-8339
[Abstract]
[Full Text]
-
Lu, Y. E., Kielian, M.
(2000). Semliki Forest Virus Budding: Assay, Mechanisms, and Cholesterol Requirement. J. Virol.
74: 7708-7719
[Abstract]
[Full Text]
-
Gibbons, D. L., Ahn, A., Chatterjee, P. K., Kielian, M.
(2000). Formation and Characterization of the Trimeric Form of the Fusion Protein of Semliki Forest Virus. J. Virol.
74: 7772-7780
[Abstract]
[Full Text]
-
Chatterjee, P. K., Vashishtha, M., Kielian, M.
(2000). Biochemical Consequences of a Mutation That Controls the Cholesterol Dependence of Semliki Forest Virus Fusion. J. Virol.
74: 1623-1631
[Abstract]
[Full Text]
-
Ahn, A., Klimjack, M. R., Chatterjee, P. K., Kielian, M.
(1999). An Epitope of the Semliki Forest Virus Fusion Protein Exposed during Virus-Membrane Fusion. J. Virol.
73: 10029-10039
[Abstract]
[Full Text]